Impact of Pyrolysis Temperature and Feedstock on Surface Charge and Functional Group Chemistry of Biochars

The capacity of biochars to adsorb ionic contaminants is strongly influenced by biochar surface chemistry. We studied the effects of biomass feedstock type, pyrolysis temperature, reaction media pH, and AlCl 3 pre‐pyrolysis feedstock treatments on biochar anion exchange capacity (AEC), cation exchange capacity (CEC), point of zero net charge (PZNC), and point of zero salt effect (PZSE). We used the relationship between PZNC and PZSE to probe biochar surfaces for the presence of unstable (hydrolyzable) surface charge functional groups. The results indicate that biochars produced at ≤500°C have high CECs and low AEC, PZSE, and PZNC values due to the dominance of negative surface charge arising from carboxylate and phenolate functional groups. Biochars produced at ≥700°C have low CEC and high AEC, PZSE, and PZNC values, consistent with a dominance of positive surface charge arising from nonhydrolyzable bridging oxonium (oxygen heterocycles) groups. However, biochars produced at moderate temperatures (500–700°C) have high PZSE and low PZNC values, indicating the presence of nonbridging oxonium groups, which are rapidly degraded under alkaline conditions by OH − attack on the oxonium α‐C. Biochars treated with AlCl 3 have high AEC, PZSE, and PZNC values due to variably charged aluminol groups on biochar surfaces. The results provide support for the presence of both hydrolyzable and nonhydrolyzable oxonium groups on biochar surfaces. They also demonstrate that biochars produced at high pyrolysis temperatures (>700°C) or those receiving pre‐pyrolysis treatments with AlCl 3 are optimized for anionic contaminant adsorption, whereas biochars produced at low pyrolysis temperatures (400°C) are optimized for cationic contaminant adsorption. Core Ideass Feedstock and pyrolysis temperature strongly affect biochar surface charges. Carboxylic and phenolic functional groups contribute surface charges of ≤500°C biochar. Nonbridging oxonium ions declined at high pyrolysis temperature. Alkaline condition of media degraded the number of nonbridging oxonium ions. Aluminol groups contribute variable charges of Al‐modified biochars.